A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220277



Internal ID20787317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78726767..78767527hg38UCSC Ensembl
chr8:79639002..79679762hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3840761
hg1940761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424479
Supporting Variants
Samples
Known GenesIL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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